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Identification of the molecular etiology in congenital hemolytic anemias beyond hemoglobinopathies using a targeted next-generation sequencing panel

dc.contributor.authorALBAYRAK, CANAN
dc.contributor.authorEKER, İBRAHİM
dc.contributor.authorKARADAŞ, NİHAL
dc.contributor.authorSARPER, NAZAN
dc.contributor.authorOymak, Yesim
dc.contributor.authorATİK, TAHİR
dc.contributor.authorIŞIK, ESRA
dc.contributor.authorAYDINOK, YEŞİM
dc.contributor.authorOrhan, Mehmet Fatih
dc.contributor.authorKarakas, Zeynep
dc.contributor.authorÖZKINAY, FERİŞTAH FERDA
dc.contributor.authorÇOĞULU, MUHSİN ÖZGÜR
dc.contributor.authorÜNAL, SELMA
dc.date.accessioned2022-07-04T12:23:48Z
dc.date.available2022-07-04T12:23:48Z
dc.date.issued2022
dc.identifier.citationATİK T., IŞIK E., AYDINOK Y., Orhan M. F. , Oymak Y., Karakas Z., SARPER N., ALBAYRAK C., KARADAŞ N., EKER İ., et al., "Identification of the molecular etiology in congenital hemolytic anemias beyond hemoglobinopathies using a targeted next-generation sequencing panel", EUROPEAN JOURNAL OF HUMAN GENETICS, cilt.30, sa.SUPPL 1, ss.221, 2022
dc.identifier.issn1018-4813
dc.identifier.otherav_1a387e64-56df-49fe-bfde-62bbefa44102
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/181800
dc.language.isoeng
dc.subjectDrug Discovery
dc.subjectAging
dc.subjectGeneral Biochemistry, Genetics and Molecular Biology
dc.subjectBiochemistry
dc.subjectStructural Biology
dc.subjectGenetics (clinical)
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectBiochemistry, Genetics and Molecular Biology (miscellaneous)
dc.subjectGenetics
dc.subjectClinical Biochemistry
dc.subjectCancer Research
dc.subjectMolecular Biology
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.titleIdentification of the molecular etiology in congenital hemolytic anemias beyond hemoglobinopathies using a targeted next-generation sequencing panel
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF HUMAN GENETICS
dc.contributor.departmentEge Üniversitesi , Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.identifier.volume30
dc.identifier.issueSUPPL 1
dc.identifier.startpage221
dc.identifier.endpage221
dc.contributor.firstauthorID3417032


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